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D-loop somatic mutations and similar to 5 kb 'common' deletion in mitochondrial DNA: important molecular markers to distinguish oral precancer and cancer

机译:线粒体DNA中的D环体细胞突变和类似于5 kb的“常见”缺失:区分口腔癌前和癌症的重要分子标记

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摘要

Apart from genomic DNA, mutations at mitochondrial DNA (mtDNA) have been hypothesized to play vital roles in cancer development. In this study, similar to 5 kb deletion and D-loop mutations in mtDNA and alteration in mtDNA content were investigated in buccal smears from 104 healthy controls and 74 leukoplakia and 117 cancer tissue samples using Taqman-based quantitative assay and re-sequencing. The similar to 5 kb deletion in mtDNA was significantly less (9.8 and 10.5 folds, P<0.0001) in cancer tissues compared to control and leukoplakia tissues, respectively. On the other hand, somatic mutations in D-loop, investigated in 54 controls, 50 leukoplakias and 56 cancer patients, were found to be significantly more in cancer tissues, but not in leukoplakia tissues, compared to control (Z-score=5.4). MtDNA contents were observed to be significantly more in leukoplakia (2.1 folds, P=0.004) and cancer (1.6 folds, P=0.03) tissues compared to control tissues. So, D-loop somatic mutations and similar to 5 kb deletion patterns could be used as distinguishing markers between precancer and cancer tissues. This observation further suggests that somatic mutations in D-loop may facilitate carcinogenesis and cancer cells with less similar to 5 kb deletion, i.e., intact mtDNA, may become resistant to apoptosis.
机译:除了基因组DNA,线粒体DNA(mtDNA)的突变被认为在癌症发展中起着至关重要的作用。在这项研究中,使用基于Taqman的定量分析和重新测序方法,对104例健康对照者和74例白斑和117例癌组织样本的口腔涂片中类似的mtDNA 5 kb缺失和D环突变以及mtDNA含量变化进行了研究。与对照组和白斑组织相比,在癌组织中与mtDNA相似的5 kb缺失分别明显更少(9.8和10.5倍,P <0.0001)。另一方面,与对照组相比,在54位对照,50位白斑和56位癌症患者中进行了研究,发现D环的体细胞突变明显多于癌组织,但在白斑组织中则没有(Z评分= 5.4) 。与对照组相比,在白斑(2.1倍,P = 0.004)和癌症(1.6倍,P = 0.03)组织中,MtDNA含量明显更高。因此,D环体细胞突变和类似的5 kb删除模式可以用作癌前组织和癌组织之间的区分标记。该观察结果进一步表明,D-环中的体细胞突变可以促进癌变,并且具有较少类似于5kb缺失的癌细胞,即完整的mtDNA,可以对细胞凋亡具有抗性。

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